Collecting cells from people with rare cystic fibrosis mutations

This is a research study that collects cells and blood samples from people with cystic fibrosis who carry rare mutations in their CFTR gene. The researchers are building a collection of these samples to study how rare mutations affect the disease and potentially develop better treatments in the future. No experimental drugs or treatments are involved—this is simply a cell and tissue collection study.

Most cystic fibrosis research focuses on common mutations, leaving people with rare mutations with fewer treatment options and less scientific understanding of their condition. By collecting and studying cells from people with these rare mutations, researchers hope to better understand how different mutations affect the disease and eventually create more personalized treatments.